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The Efficacy of Botulinum Toxin Alone Versus Combined Botulinum Toxin and Topical Diltiazem in Chronic Anal Fissure

M

Medipol Health Group

Status

Completed

Conditions

Anal Fissure Chronic

Treatments

Drug: Botulinum Toxin Type A Injection [Botox]
Drug: Botulinum Toxin Type A Injection [Botox] + Diltiazem Hydrochloride 20 Mg/G Rectal Gel

Study type

Observational

Funder types

Other

Identifiers

NCT05797220
E-10840098-772.02-786

Details and patient eligibility

About

Anal fissure (AF) is a painful tear extending from the anal canal to the dentate line. Although the exact pathophysiology is not known, an increase in anal tonus, decreased ano-dermal blood flow and local ischemia are possible mechanisms. The most effective treatment modality in chronic AF is lateral internal sphincterotomy however, incontinence rates are still reported as high as 8-30%. Topical diltiazem and botulinum toxin (BT) injection are good alternatives to surgery with lack of persistent side effects, easy applicability, and reproducibility, however, recurrence rates were reported up to 50% for each. A combination of BT with topical diltiazem may provide better results in terms of healing and recurrence. In this retrospective analysis a comparison of BT injection alone and BT injection combined with topical diltiazem treatment was performed.

Enrollment

217 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with complaints longer than 8 weeks (chronic anal fissure)
  • Patients who completed at least 24 months of follow-up (3rd day, 10th day, 1st-month, and 2nd-month face-to-face clinic visits and 6, 12, and 24 months phone calls)
  • Patients who received conservative treatments including topical diltiazem and nitrites

Exclusion criteria

  • Patients with previous anal surgery (lateral internal sphincterotomy, hemorrhoidectomy, anal fistula)
  • Patients with inflammatory bowel diseases
  • Patients with accompanying anorectal disease (hemorrhoids, anal fistula, abscess)
  • Patients who underwent botulinum toxin injection within 1 year before recruitment
  • Patients with anterior, lateral, or multiple fissures
  • Comorbidities (AIDS, sexually transmitted disease, tuberculosis, leukemia)
  • Pregnancy
  • Prescription of calcium canal blockers or nitrites
  • Hypersensitivity to diltiazem or botulinum toxin
  • Patients without anal pain

Trial design

217 participants in 2 patient groups

Botulinum toxin group
Description:
The procedures were performed at outpatient clinic without anesthesia. Lyophilized 100 IU BT Type-A (BOTOX, Alergan, CA, USA) was applied after diluted with 1 cc saline. A 26-G injector was used to inject 25 unit toxin in every 4 quadrants, to the alignment of clock 12, 3, 6, and 9 to internal anal sphincters.
Treatment:
Drug: Botulinum Toxin Type A Injection [Botox]
Botulinum toxin plus topical diltiazem group
Description:
The procedures were performed at outpatient clinic without anesthesia. Lyophilized 100 IU BT Type-A (BOTOX, Alergan, CA, USA) was applied after diluted with 1 cc saline. A 26-G injector was used to inject 25 unit toxin in every 4 quadrants, to the alignment of clock 12, 3, 6, and 9 to internal anal sphincters. After BT injection, topical 2% diltiazem gel was prescribed, applied 2 times per day for 10 days (2 doses of 1 gr each per day). No selection criteria were used when recommending this treatment; it was randomly suggested to some for a while during the cohort since the surgeon believed it might enhance the efficacy of BT.
Treatment:
Drug: Botulinum Toxin Type A Injection [Botox] + Diltiazem Hydrochloride 20 Mg/G Rectal Gel

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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